Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71166생성일: 2026년 10월 23일
3-Carbethoxy-2-piperidone → ethyl 3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine-8-carboxylate
https://huagongshe.com/ko/reaction/71166
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 3-Carbethoxy-2-piperidone | HCID 97773 | — |
| 반응물 | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| 반응물 | 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzohydrazide | HCID 66607850 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | ethyl 3-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridine-8-carboxylate | HCID 66608063 | 38.2% |
반응 단계
To a mixture of ethyl 2-oxopiperidine-3-carboxylate (1.86 g) in acetonitrile (20 mL) was added trimethyloxonium tetrafluoroborate (1.61 g) at room temperature, and the mixture was stirred at room temperature for 2 hr. 3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)benzohydrazide (2.23 g) was added to the reaction mixture at room temperature, and the mixture was heated under reflux for 2 hr. The reaction mixture was allowed to cool to room temperature, and diluted with ethyl acetate and saturated aqueous sodium hydrogen carbonate solution, the mixture was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was collected by filtration, and washed with ethyl acetate to give the title compound (1.32 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822699B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-6a3e7fab210146a481e15b7772ff17ba |
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| 출처 메모 | uspto-grants-2014_09 |
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